FDA 510(k) Applications Submitted by GERMAINE LABORATORIES, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K013857 |
11/21/2001 |
AIMSTEP PREGNANCY |
GERMAINE LABORATORIES, INC. |
| K980531 |
02/11/1998 |
AIMSTEP PREGNANCY |
GERMAINE LABORATORIES, INC. |
| K981165 |
03/31/1998 |
AIMSTEP COMBO PREGNANCY, 1 TEST, 30 TEST, 50 TEST, 100 TEST |
GERMAINE LABORATORIES, INC. |
| K991369 |
04/20/1999 |
ACCUDIP HOME PREGNANCY AND/OR AIMSTICK PREGNANCY |
GERMAINE LABORATORIES, INC. |
| K051727 |
06/28/2005 |
AIMSTICK URINE REAGENT STRIPS |
GERMAINE LABORATORIES, INC. |
| K973825 |
10/07/1997 |
MIDSTREAM HOME REGNANCY TEST |
GERMAINE LABORATORIES, INC. |
| K974368 |
11/20/1997 |
AIMSTICK PBD PREGNANCY |
GERMAINE LABORATORIES, INC. |
| K974512 |
12/01/1997 |
AIMSTICK PBD COMBO PREGNANCY |
GERMAINE LABORATORIES, INC. |
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